Senior Project Manager, R&D

Company OverviewEmbark on an enriching journey with PROCEPT BioRobotics, where our vision, mission, and values guide everything we do as a company. At PROCEPT, we put the patient first in everything we do and are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH, otherwise known as prostate gland enlargement) through innovation in surgical robotics. As our company succeeds and grows, we improve the quality of life of patients, provide more effective treatment options for surgeons, uphold the trust of our shareholders. That starts with a commitment to our People with a focus on creating an evolving landscape for your career, brimming with transformative opportunities that provide continuous career growth opportunities.
The Opportunity That Awaits You:   
The Senior Project Manager in the Research and Development Department is the glue between the cross functional teams that drives projects from start to finish. This role is an integral part of the PROCEPT R&D team and the face of the program for the business. The project manager is responsible for developing, managing, and ensuring that the program schedule and CFT deliverables are hit with the quality that PROCEPT stands for. They are involved in all aspects of the project from initial planning to technical reviews to status updates and schedule mitigation planning. The Project Manager role oversees all initiatives going on for the program and is responsible for driving cross-functional alignment on deliverables, ensuring compliance activities are performed, managing risks, defining project scopes, objectives and timelines and aligning resource allocation to meet needs. This is not a “schedule jockey”– the Project Manager is expected to use their own technical expertise and judgement to help set plans, flag / resolve misalignment, identify trade-offs when necessary and ensure a quality deliverable is made on time.The successful candidate will have a proven track record working as part of / with cross functional teams including development, operations, regulatory, quality, and commercial. They have a “hands on” personality to learn, get involved, and support the program where needed. Previous experience as an engineer with cross-functional experience will enable this project manager to be successful with planning and working with the teams.  Key skills include strong communication, cross-functional collaboration, attention to detail and willingness to dive in, ability to extrapolate, ability to juggle many tasks at any point in time without dropping any one of them. The successful candidate will be one who provides great value to the teams while ensuring their successful alignment with the broader company.

What Your Day-To-Day Will Involve:

• Drive cross-functional alignment across cross functional You will do this by extreme communication, experience doing the deliverables, and having a clear eye on the prize – high quality, on schedule product. Keep people focused, identify and knock down blockers, ensure alignment, propose trade-offs.
• Keep multiple independent and dependent projects on track, ensuring priorities are clearly set and next steps are clearly communicated.
• Use your technical, clinical and/or product knowledge to pressure-test proposals, requirements, and specifications, acting as a critical reviewer and a sanity checker. Work with various teams to define requirements.
• Identify and manage project and technical risks, dependencies and mitigation strategies.
• Ensure design controls & quality processes are followed and appropriate documentation is available at the right time. Proactively create and/or drive documentation ahead of deadlines.
• Organize & lead meetings to accomplish the above, while communicating to keep people aligned and on schedule.
• Actively seek out and propose ways to improve how PROCEPT works – ask “Why?” and “Why not?” whenever possible. 

The Qualifications We Need You to Possess

• Proven experience managing complex programs, developing program schedules, identifying areas or risk and areas of buffer. Comfortable pressure testing team members and leveraging engineering experience to optimize how things are completed.
• Extensive collaboration, communication & organizational skills across extended teams. Experience preparing and giving executive summaries / reports
• Familiarity/experience working in a regulated domain. Prefer experience in medical device industry including familiarity with IEC 62304, ISO 13485, FDA device regulations & QSR, MD-SAP, IEC 81001-5-1.
• Ability to move quickly in a fast-paced environment, adapt to changing conditions and create clarity out of chaos. 

The Qualifications We Would Like You to Pos